Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048117Generated: November 2, 2026

Potassium Phosphate, Tribasic → HCID 58042453, compound

https://huagongshe.com/reaction/2048117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
ReactantCyclopropylboronic acidHCID 2760897—
ReactantHCID 58042400HCID 58042400—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 58042453HCID 5804245343%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Bromo-3-(1,1-difluoroethoxy)pyridine (Preparation 266, 700 mg, 2.948 mmol), cycloproyl boronic acid (252 mg, 2.94 mmol), and potassium phosphate tribasic (1.56 g, 7.35 mmol) were suspended in a mixture of toluene (100 mL) and water (20 mL), with rapid stirring. The suspension was heated to 80° C., and the solvent de-gassed by direct bubbling of N2 gas through the suspension for 30 minutes. The reaction was then heated to 95° C., and tricyclohexyl phosphine (82 mg, 0.29 mmol), rapidly followed by palladium acetate (33 mg, 0.15 mmol), were added. The reaction was left to stir and heat at 95° C. for 18 hours. The reaction was cooled to room temperature, and filtered through a plug of arbocel, eluting with ethyl acetate. The solvent was removed to leave a dark yellow oil. Ethyl acetate was added (100 mL), and the organic phase extracted with 2M HCl solution (3×100 mL). The organic phase was discarded. Ethyl acetate (150 mL) was added to the combined aqueous layers, and solid sodium bicarbonate was added until the aqueous layer reached pH 7. The mixture was transferred to a separating funnel, the organic layer was removed and the aqueous layer was extracted with ethyl acetate (2×100 mL). The combined organic phases were dried over magnesium sulfate, filtered and the solvent removed to leave a yellow oil. The material was purified by silica gel column chromatography eluting with 1:1 heptane:ethyl acetate to afford the title compound as a colourless oil (252 mg, 43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592629B2
Source datasetuspto-grants-2013_11
ORD IDord-98378a34d1a44aa7ba500614d5db8ecd
Source noteuspto-grants-2013_11